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Effective June 18, 2014 - Turn onto Ashland Ave from Broadway, to access the Kennedy Krieger parking garage. Please allow more time for travel to appointments.
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Devin S. Gary, Ph.D.
Kennedy Krieger Institute
707 N. Broadway
Baltimore, MD 21205
Phone: (443) 923-9246
Trained in neuroscience and neuroanatomy, Dr. Gary oversees research in the laboratory in the International Center for Spinal Cord Injury at Kennedy Krieger Institute.
Dr. Devin Gary received his doctorate in 2002 from the University of Kentucky after dual training at UK and the National Institute on Aging at Johns Hopkins Bayview Campus under the direction of Dr. Mark Mattson. After three years post-doctoral training in the Department of Neuropathology at Johns Hopkins with Dr. David Borchelt, Dr. Gary joined the International Center for Spinal Cord Injury at Kennedy Krieger Institute as a faculty instructor to work with Dr. John McDonald. Dr. Gary currently oversees research on spinal cord injury in the ICSCI laboratory.
Traumatic spinal cord injury (SCI) is a devastating condition resulting in cell death of neural tissue, interruption of ascending and descending tracts and loss of myelin. The use of transplanted cells to reduce or replace cell loss (i.e., neurons and glia) in the spinal cord is a major focus of current research in the SCI field. Emphasis in this area has been placed on the use of cells to deliver trophic support to tissue (e.g., growth factor expression), the use of neuronal progenitors to replace lost motor or sensory function and the use of oligodendrocyte progenitors to replace myelin.
While it is likely that some combination of all these approaches may be needed to achieve a true therapeutic tool in cell transplantation therapy, we still know very little about the impact of the injured cord's environment on the transplanted cells' survival, differentiation or integration. In addition, how transplanted cells actually promote recovery of function following SCI is still an open area of investigation.
Dr. Gary’s research involves approaches aimed at understanding the mechanisms and role of remyelination following spinal cord injury. This work focuses on remyelination from both endogenous oligodendrocyte progenitor cells and transplanted embryonic stem (ES) cell-derived oligodendrocytes. Previous research suggests that functional remyelination, even in modest amounts, can translate into tremendous gain of function following spinal cord injury. Using mouse ES cells as a tool, Dr. Gary is addressing the best ways to achieve remyelination following spinal cord injury.